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EIF4H has two isoforms. The short isoform (~25kDa) is the predominant isoform and is expressed alone in liver and skeletal muscle. This is a rabbit anti-EIF4H polyclonal antibody raised against part of N-terminal chain of human EIF4H, and can recognize both isoforms.
Immunogen sequence: MADFDTYDD RAYSSFGGGR GSRGSAGGHG SRSQKELPTE PPYTAYVGNL PFNTVQGDID AIFKDLSIRS VRLVRDKDTD KFKGFCYVEF DEVDSLKEAL TYDGALLGDR SLRVDIAEGR KQDKGGFGFR KGGPDDRGFR DDFLGGRGGS RPGDRRTGPP MGSRFRDGPP LRGSNMDFRE PTEEERAQR (1-188 aa encoded by BC010021 )
This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: eIF-4H; Eukaryotic translation initiation factor 4H; Williams-Beuren syndrome chromosomal region 1 protein; Williams-Beuren syndrome chromosome region 1
Gene Aliases: eIF-4H; EIF4H; KIAA0038; WBSCR1; WSCR1
UniProt ID: (Human) Q15056
Entrez Gene ID: (Human) 7458
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